作者: Robert A. Avery , James A. Katowitz , Michael J. Fisher , Gena Heidary , Eva Dombi
DOI: 10.1016/J.OPHTHA.2016.09.020
关键词:
摘要: Topic Children and adults with neurofibromatosis type 1 (NF1), a common autosomal dominant condition, manifest a variety of ophthalmologic conditions. Plexiform neurofibromas (PNs) involving the eyelid, orbit, periorbital, and facial structures (orbital-periorbital plexiform neurofibroma [OPPN]) can result in significant visual loss in children. Equally important, OPPNs can cause significant alteration in physical appearance secondary to proptosis, ptosis, and facial disfigurement, leading to social embarrassment …